HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Aminophenol → 2-(1-Methylpentylamino)phenol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Aminophenol | HCID 5801 | — |
| Reactant | 2-Hexanone | HCID 11583 | — |
| Product | 2-(1-Methylpentylamino)phenol | HCID 23106862 | — |
Reaction Steps
The same procedure as in Example 3 was repeated except for using 145 mL (121 g; 1.2 mol) of 2-hexanone in place of 100 mL of acetone, to conduct the reaction. As a result, it was confirmed that the rate of conversion of o-aminophenol was 93%, the selectivity to the N-monoalkylated compound (molar ratio of the monoalkylated compound to a sum of the mono- and di-alkylated compounds) was 41%, and the oxygen absorption initiation time as an index of determining an oxidation-inhibiting property thereof was 320 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07498467B2 |
| Source dataset | uspto-grants-2009_03 |
| ORD ID | ord-15517788c82a494ab29657e4fdbb073d |
| Source note | uspto-grants-2009_03 |